Canonical Allele Identifier: PA2825495626
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 453823
ClinVar RCV Id: RCV000544815 RCV002448594 RCV002481742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077072.1:p.Met802Thr
CA374114313
NM_001083603.3:c.2405T>C