Canonical Allele Identifier: PA2825507864
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 216381
ClinVar RCV Id: RCV000196599 RCV001020163 RCV003441778
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077074.1:p.Ala979Thr
CA336551
NM_001083605.3:c.2935G>A