Canonical Allele Identifier: PA2825507808
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 547923
ClinVar RCV Id: RCV000660493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077074.1:p.Phe953Leu
CA374111923
NM_001083605.3:c.2859T>G
CA374111924
NM_001083605.3:c.2859T>A
CA374111930
NM_001083605.3:c.2857T>C