Canonical Allele Identifier: PA2825492287
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2911465
ClinVar RCV Id: RCV003609785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077072.1:p.Thr210Ser
CA374115060
NM_001083603.3:c.628A>T